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Notifications: to remind you of their appointments and inform them if other clinical studies are available near them.
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Mobile/tablet friendly
web application.
Clinical trials are a fundamental part of medical research that aims to find new ways to prevent, detect or treat diseases. These new treatments can be new molecules, combinations of different molecules, new ways of administering them, new treatment techniques (surgery, radiotherapy). The goal of clinical trials is to improve the treatment of patients at all stages of the disease. They allow us to evaluate the effectiveness and tolerance of new treatments before they are put on the market. When you participate in clinical research, you help doctors and researchers learn more about diseases and find alternative treatments for your disease.
As an IBD patient, you have probably done a lot of research about your disease and its different stages, you have explored several websites and forums in search of answers, support or simply to exchange information. Telemedicine Technologies puts at your disposal the afa website that you can consult through the following link. afa is the only French association that supports and informs Crohn’s and ulcerative colitis patients and their relatives, defends their rights, and finances research.
Access ToTem4meWe understand the difficulties you are going through and the obstacles you face in finding clinical trials that are right for you. At Telemedicine Technologies, we support you and are actively working with physicians and patients (through the afa) to provide you with easy access to clinical trials near you so that you can find the innovative treatments you want and deserve. in a few clicks and minutes wherever you are! in total security!
Access ToTem4meOn-line Patient Questionnaire
Connect to the ToTem4me application, fill out a questionnaire in 2 minutes, and find out if there are ongoing clinical trials in your area of choice that could potentially suit you.
Coordinator interview & study identification
The expert coordinator finetunes with you the identification of potential study(ies), explains clinical studies typical process, and confirms your interest.
Site
referral
The expert coordinator forwards your contact details to the hospital you select, so that an appointment is given to you. The investigational team confirms your potential eligibility and initiate the screening.
Patient
follow-up
The expert coordinator follows-up with the investigational team to ascertain that you had your appointment and enquires on the follow-up proposed.
Your data is never shared with a trial site You have the right to be forgotten and have your data fully deleted. the coordinator has no access to your personnal datas Only limited information is captured to protect your privacy ToTem4me is GDPR compliant
June 27, 2024
25 September 2024 from 4:00PM to 5:30PM (CEST) Webinar Overview It has been demonstrated that using standards from the start of clinical research studies (i.e. protocol and CRF development) can save significant time and resources and results in higher quality research. Unfortunately, it is not always clear how to select the appropriate standards for the […]
June 27, 2024
Applied Clinical Trials Online ACT: How can data management challenges be addressed? Specifically, is there any opportunity to address them with artificial intelligence (AI)? Lacroix: There is a lot of opportunity across the life cycle to assist with this and it’s interesting because historically it was always: we want to throw people at some of […]
June 27, 2024
Fiercebiotech Experts recommend that CGT manufacturers proactively design a comprehensive market access strategy early in clinical development and commercial planning timelines, ideally more than three years prior to launch. This strategy should focus on addressing the nuanced market access challenges for such treatments, including but not limited to, distribution network design, tailored commercial site engagement, […]